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A hierarchical structured composite made from clinoptilolite supported on date stones carbon is synthesized using two techniques. The composites are manufactured by fixing a natural zeolite (clinoptilolite) to the porous surface of date stones carbon or by direct hydrothermal synthesis on to the surface to provide a supported high surface area ion-exchange material for metal ion removal from aqueous streams. The fixing of the clinoptilolite is achieved using sucrose and citric acid as a binder. The composites and pure clinoptilolite were compared to test the efficacy for the removal of Sr 2+ ions from an aqueous phase. The encapsulation of the Sr 2+ using either vitrification or a geo-polymer addition was tested to ensure that the hazardous waste can be made safe for disposal. The hierarchical structured composites were shown to achieve a higher ion exchange capacity per gram of zeolite than the pure clinoptilolite (65 mg/g for the pure natural clinoptilolite and 72 mg/g for the pure synthesized clinoptilolite) with the synthesized composite (160 mg/g) having higher capacity than the natural clinoptilolite composite (95 mg/g). The rate at which the equilibria were established followed the same trend showing the composite structure facilitates diffusion to the ion-exchange sites in the zeolite. [ABSTRACT FROM AUTHOR]

Recent research has demonstrated a new synthesis route for hierarchically porous zeolite composites by mechanical modification of the support surface using ultrasonication in a nanoparticle suspension. It was believed that target zeolites should be added as seeds for the sonication. In this study, the effect of nanoparticles was investigated with ultrasonication to understand the crystallization mechanism of zeolites obtained by the nanoparticles–assisted synthesis. It has been found that the nanoparticles under the influence of ultrasonication generate fissures or cracks as nucleation sites on the carbon surface. These nanoparticles such as zeolite A, γ-Al 2 O 3 , quartz and sand are different from the target zeolite X. Therefore, an amorphous aluminosilicate gel nucleates at those cracks during the hydrothermal treatment. Thus, the mechanical activation of the support surface is the process to induce the formation of strongly attached zeolite X over the template, not a seeding step. This is confirmed as an attachment due to the weak bond between the support and the zeolite for ‘non-seeded’ composites whereas the ‘seeded’ composites have a robust structure which maintains a zeolite coating upon mechanical agitation. [ABSTRACT FROM AUTHOR]

In this work, composite membranes for a direct methanol fuel cell (DMFC) were prepared using a spraying method to improve cell performance especially at a high methanol concentration. Nafion polymer and mordenite as a filler were used for the composite membrane preparation using a spraying method and a conventional solution casting method and the membranes from the two methods were compared. SEM images showed that a more homogeneous composite membrane could be obtained using the spraying method. The effect of mordenite content was also studied. The membranes were consequently characterized and tested in DMFC operation. The results were compared to those prepared using the solution casting method at 30, 50, and 70 °C with methanol concentrations of 2, 4, and 8 M. It was found that the membrane with 5 wt.% mordenite from the spraying method showed a vast improvement in DMFC performance. When the cell was operated at 70 °C, the maximum power density of 5 wt.% mordenite from the spraying method was higher than that of commercial membrane and 5 wt.% from the solution casting method. Power densities from the 5 wt.% sprayed membrane were higher by around 29%, 40%, and 60% at 2, 4, and 8 M methanol concentration, respectively. [ABSTRACT FROM AUTHOR]

Abstract: Composite polymer proton exchange membranes (PEM) were prepared by solution recasting. The composite membranes formed are based on Nafion incorporating a silane functionalized zeolite, mordenite, as an additive. The composite membranes were placed within a single cell DMFC and compared to an MEA featuring a standard Nafion 125μm membrane. The impact of mordenite particle size, the choice of the silane functionalizing agent and the membrane preparation procedure are investigated. A composite ion exchange membrane which featured Nafion and a ground mordenite which was functionalized using glycidoxypropyltrimethoxysilane achieved a power density that outperformed a standard Nafion MEA under all conditions. [Copyright &y& Elsevier]